Barth syndrome mutations that cause tafazzin complex lability

Authors

Steven M. Claypool, Johns Hopkins School of Medicine
Kevin Whited, Johns Hopkins School of Medicine
Santi Srijumnong, University of California, Los Angeles
Xianlin Han, Washington University School of Medicine in St. Louis
Carla M. Koehler, University of California, Los Angeles

Journal

Journal of Cell Biology

Publication Date

2011

Volume

192

Issue

3

First Page

447

Last Page

462

Document Type

Open Access Publication

DOI

10.1083/jcb.201008177

Rights and Permissions

Claypool SM, Whited K, Srijumnong S, Han X, Koehler CM. Barth syndrome mutations that cause tafazzin complex lability. J Cell Biol. 2011 Feb 7;192(3):447-62. doi: 10.1083/jcb.201008177. © 2011 Claypool et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).

Recommended Citation

Claypool, Steven M.; Whited, Kevin; Srijumnong, Santi; Han, Xianlin; and Koehler, Carla M., "Barth syndrome mutations that cause tafazzin complex lability." Journal of Cell Biology. 192, 3. 447 - 462. (2011).
https://digitalcommons.wustl.edu/open_access_pubs/8552